<?xml version="1.0" encoding="UTF-8"?>
<eudamedExport entity="devices">
  <row>
    <udiDi>D-80565185095375K</udiDi>
    <basicUdiDi>B-80565185095375K</basicUdiDi>
    <tradeName>BIOCOLLAGEN®</tradeName>
    <deviceName>BIOCOLLAGEN® Collagen fleece</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BCG-200</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:55.875Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850952052</udiDi>
    <basicUdiDi>B-805651850952052</basicUdiDi>
    <tradeName>BIOCOLLAGEN®</tradeName>
    <deviceName>BIOCOLLAGEN® Collagen fleece</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BCG-255</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:55.072Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850951355</udiDi>
    <basicUdiDi>B-805651850951355</basicUdiDi>
    <tradeName>BIOCOLLAGEN®</tradeName>
    <deviceName>BIOCOLLAGEN® Collagen fleece</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BCG-1008</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:51.078Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850950658</udiDi>
    <basicUdiDi>B-805651850950658</basicUdiDi>
    <tradeName>OSTEOPLANT® Flex</tradeName>
    <deviceName>OSTEOPLANT® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OTC-CE2</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:50.280Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185094835M</udiDi>
    <basicUdiDi>B-80565185094835M</basicUdiDi>
    <tradeName>OSTEOPLANT® Flex</tradeName>
    <deviceName>OSTEOPLANT® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OTC-C3</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:48.674Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185094695T</udiDi>
    <basicUdiDi>B-80565185094695T</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous block</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-OX55</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:43.869Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185094525A</udiDi>
    <basicUdiDi>B-80565185094525A</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous block</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-OX54</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:43.074Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185094455D</udiDi>
    <basicUdiDi>B-80565185094455D</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Cancellous cortical mix gel</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-OX22</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:42.273Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185094214X</udiDi>
    <basicUdiDi>B-80565185094214X</basicUdiDi>
    <tradeName>OSTEOXENON® Flex</tradeName>
    <deviceName>OSTEOXENON® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-OX04</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:37.479Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850941452</udiDi>
    <basicUdiDi>B-805651850941452</basicUdiDi>
    <tradeName>OSTEOXENON®</tradeName>
    <deviceName>OSTEOXENON® Flex cortical sheet</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OSP-OX02A</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:36.674Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850940755</udiDi>
    <basicUdiDi>B-805651850940755</basicUdiDi>
    <tradeName>OSTEOPLANT®</tradeName>
    <deviceName>OSTEOPLANT® Cancellous block</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OMC-50b</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:35.869Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093915F</udiDi>
    <basicUdiDi>B-80565185093915F</basicUdiDi>
    <tradeName>CALCITOS®</tradeName>
    <deviceName>CALCITOS® Cancellous granules</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OMC-030</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:31.867Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093775M</udiDi>
    <basicUdiDi>B-80565185093775M</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OGS-ACM600</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:30.264Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850936054</udiDi>
    <basicUdiDi>B-805651850936054</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM mouldable paste</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OGS-ACM500</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:29.465Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850935357</udiDi>
    <basicUdiDi>B-805651850935357</basicUdiDi>
    <tradeName>OSTEOPLANT® ACTIVAGEN®</tradeName>
    <deviceName>OSTEOPLANT® ACTIVAGEN® DBM granules</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>OGS-AC5</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:25.458Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093465A</udiDi>
    <basicUdiDi>B-80565185093465A</basicUdiDi>
    <tradeName>HEART®</tradeName>
    <deviceName>HEART® Pericardium membrane</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>HRT-005</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:24.654Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093395D</udiDi>
    <basicUdiDi>B-80565185093395D</basicUdiDi>
    <tradeName>HEART®</tradeName>
    <deviceName>HEART® Pericardium membrane</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>HRT-003</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:23.857Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093224U</udiDi>
    <basicUdiDi>B-80565185093224U</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous granules</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BGS-23</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:23.056Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-80565185093154X</udiDi>
    <basicUdiDi>B-80565185093154X</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous granules</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BGS-22</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:19.052Z</lastUpdated>
  </row>
  <row>
    <udiDi>D-805651850930852</udiDi>
    <basicUdiDi>B-805651850930852</basicUdiDi>
    <tradeName>BIO-GEN®</tradeName>
    <deviceName>BIO-GEN® Cancellous granules</deviceName>
    <manufacturerName>BIOTECK S.p.A.</manufacturerName>
    <manufacturerSrn>IT-MF-000011484</manufacturerSrn>
    <authorisedRepresentativeName></authorisedRepresentativeName>
    <authorisedRepresentativeSrn></authorisedRepresentativeSrn>
    <riskClass>Sınıf III</riskClass>
    <legislation>MDD</legislation>
    <emdnCode>P900401</emdnCode>
    <emdnDescription>BONE AND TENDON REPLACEMENT DEVICES</emdnDescription>
    <deviceStatus>Piyasada</deviceStatus>
    <reference>BGS-21</reference>
    <placedOnMarketCountry>Italy</placedOnMarketCountry>
    <lastUpdated>2026-07-12T06:47:18.250Z</lastUpdated>
  </row>
</eudamedExport>